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Neuromuscular Dystrophy. By: Dana DeGraaf. What is Neuromuscular Dystrophy?. Neuromuscular dystrophy is a term used to refer to a group of muscle disorders in which the face, limbs, heart or spine muscles gradually weaken and shrink over time.
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Neuromuscular Dystrophy By: Dana DeGraaf
What is Neuromuscular Dystrophy? • Neuromuscular dystrophy is a term used to refer to a group of muscle disorders in which the face, limbs, heart or spine muscles gradually weaken and shrink over time. • In cases involving the heart and spine, this can be fatal.
Examples: • Duchenne muscular dystrophy • Myotonic dystrophy • Becker’s muscular dystrophy • Distal muscular dystrophy • Limb-girdle muscular dystrophy • Etc…
The different types are distinguished by factors such as: • Age at which symptoms start • Pattern of weak muscles • Speed that the disease progresses • Involvement of other tissues besides muscles • Pattern of inheritance
Causes of neuromuscular dystrophy All muscular dystrophies are inherited. Each type is associated with the genetic mutation in the DNA line. A woman who has the mutated gene is called a carrier. Each of her children have a 50% chance of getting her genetic mutation. If her child is a boy, then he will develop the muscular dystrophy. If it is a girl, she will become a carrier and have the 50% chance to pass the disease on to her children.
Signs and symptoms: • Progressive muscle wasting • Poor balance • Scolosis (curved spine) • Limited range of movement • Inability to walk
Effects on the brain: • There have been reports of a 50% decrease in neuron number and neural shrinkage in regions of the cerebral cortex and brain stem. • People diagnosed with neuromuscular dystrophy have been reported to have a lower IQ (average 85)
Thanks for watching! Sources: www.ocl.org/ www.nlm.nih.gov/ brain.oxfordjournals.org/